Canonical Allele Identifier: PA2827307871
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 946236
ClinVar RCV Id: RCV001217059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317302.1:p.Thr50Ala
CA384356230
NM_001330373.1:c.148A>G